Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:185157378-185157549 | Common:1; Rare:51 | ||||
chr1:185316757-185316863 | Rare:29 | ||||
chr1:186375104-186375523 | Rare:115 | ||||
chr1:186375557-186375932 | Common:1; Rare:110 | ||||
chr1:192808908-192809057 | Common:3; Rare:57 | ||||
chr1:193059268-193059673 | Rare:195 | ||||
chr1:193105367-193105502 | Common:2; Rare:56 | ||||
chr1:193186532-193186626 | Rare:13 | ||||
chr1:196608382-196608674 | Common:2; Rare:67 | ||||
chr1:196819567-196819902 | Common:2; Rare:37 | ||||
chr1:196887896-196888196 | Rare:66 | ||||
chr1:196943588-196943919 | Common:1; Rare:26 | ||||
chr1:196977380-196977642 | Common:1; Rare:57; Clinvar:1 | ||||
chr1:197146536-197146808 | Common:1; Rare:57; Clinvar:4; Clinvar (benign):1 | ||||
chr1:200042581-200042875 | Common:1; Rare:72 |